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ethyl α-iodophenylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78489-65-3

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78489-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78489-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,8 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78489-65:
(7*7)+(6*8)+(5*4)+(4*8)+(3*9)+(2*6)+(1*5)=193
193 % 10 = 3
So 78489-65-3 is a valid CAS Registry Number.

78489-65-3 Well-known Company Product Price

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  • CAS number
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  • TCI America

  • (E1200)  Ethyl α-Iodophenylacetate  >98.0%(HPLC)

  • 78489-65-3

  • 5g

  • 390.00CNY

  • Detail
  • TCI America

  • (E1200)  Ethyl α-Iodophenylacetate  >98.0%(HPLC)

  • 78489-65-3

  • 25g

  • 1,390.00CNY

  • Detail

78489-65-3Downstream Products

78489-65-3Relevant academic research and scientific papers

Construction of Pyrrolo[1,2-a]indoles via Cobalt(III)-Catalyzed Enaminylation of 1-(Pyrimidin-2-yl)-1H-indoles with Ketenimines and Subsequent Base-Promoted Cyclization

Zhou, Xiaorong,Fan, Zili,Zhang, Zhiyin,Lu, Ping,Wang, Yanguang

, p. 4706 - 4709 (2016/09/28)

A cobalt(III)-catalyzed cross-coupling reaction of 1-(pyrimidin-2-yl)-1H-indoles with ketenimines is reported. The reaction provided 2-enaminylated indole derivatives in moderate to excellent yields with a broad substrate scope. The prepared 2-enaminylated indoles could be conveniently converted into pyrrolo[1,2-a]indoles, which are an important class of compounds in medicinal chemistry.

Systematic study on alkyl iodide initiators in living radical polymerization with organic catalysts

Lei, Lin,Tanishima, Miho,Goto, Atsushi,Kaji, Hironori,Yamaguchi, Yu,Komatsu, Hiroto,Jitsukawa, Takuya,Miyamoto, Michihiko

, p. 6610 - 6618 (2015/02/19)

Several low-molar-mass alkyl iodides were studied as initiating dormant species in living radical polymerization with organic catalysts. Primary, secondary, and tertiary alkyl iodides with different stabilizing groups (ester, phenyl, and cyano groups) were systematically studied for the rational design of initiating alkyl iodides. The activation rate constants of these alkyl iodides were experimentally determined for quantitative comparison. These alkyl iodides were used in the polymerizations of methyl methacrylate and butyl acrylate to examine their initiation ability in these polymerizations. A telechelic polymer was prepared using an alkyl iodide with a functional group. Alkyl iodides with multi-initiating sites were also studied.

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